Molecular mechanisms underlying the oncogenic and tumor-suppressive roles of ZHX2 in cancers

IF 2.1 4区 医学 Q4 GENETICS & HEREDITY
Yifan Wei , Haiyang Guo , Jingjie Zhou , Da Shi, Liqiang Hao
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引用次数: 0

Abstract

The transcription factor ZHX2 exerts paradoxical roles in cancer, acting as either an oncogene or tumor suppressor in a context-dependent manner. This duality stems from ZHX2’s regulation of key processes including cell cycle, apoptosis, EMT, stemness, and metabolism. Consequently, ZHX2 may impacts tumor cell growth, migration, and immune evasion, positioning it as a promising therapeutic target. This short communication synthesizes current understanding of ZHX2’s molecular structure, transcriptional regulation, and its critical modulation of oncogenic and tumor-suppressive pathways across various cancers. We highlight its potential utility as a prognostic biomarker and its implications for precision medicine, chemotherapy, targeted therapy, and immunotherapy. However, translating ZHX2-targeting strategies faces significant hurdles, particularly concerning tissue-specific restoration and integration with existing treatments. Future research should prioritize overcoming these barriers and exploring ZHX2’s epigenetic regulatory potential.
肿瘤中ZHX2的致癌和肿瘤抑制作用的分子机制
转录因子ZHX2在癌症中发挥着矛盾的作用,既可以作为致癌基因,也可以作为肿瘤抑制因子。这种双重性源于ZHX2对细胞周期、凋亡、EMT、干性和代谢等关键过程的调控。因此,ZHX2可能影响肿瘤细胞的生长、迁移和免疫逃避,使其成为一个有希望的治疗靶点。这种简短的交流综合了目前对ZHX2分子结构、转录调控及其在各种癌症中致癌和肿瘤抑制途径的关键调控的理解。我们强调其作为预后生物标志物的潜在效用及其对精准医学、化疗、靶向治疗和免疫治疗的影响。然而,转化zhx2靶向策略面临着重大障碍,特别是在组织特异性修复和与现有治疗的整合方面。未来的研究应优先克服这些障碍,探索ZHX2的表观遗传调控潜力。
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来源期刊
Cancer Genetics
Cancer Genetics ONCOLOGY-GENETICS & HEREDITY
CiteScore
3.20
自引率
5.30%
发文量
167
审稿时长
27 days
期刊介绍: The aim of Cancer Genetics is to publish high quality scientific papers on the cellular, genetic and molecular aspects of cancer, including cancer predisposition and clinical diagnostic applications. Specific areas of interest include descriptions of new chromosomal, molecular or epigenetic alterations in benign and malignant diseases; novel laboratory approaches for identification and characterization of chromosomal rearrangements or genomic alterations in cancer cells; correlation of genetic changes with pathology and clinical presentation; and the molecular genetics of cancer predisposition. To reach a basic science and clinical multidisciplinary audience, we welcome original full-length articles, reviews, meeting summaries, brief reports, and letters to the editor.
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